Reported Aug 6, 2025 · Ongoing
SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
Philips North America
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips North America · 222 Jacobs St · Cambridge, MA · 02141-2296
Is this the product you have?
- SmartPath to
- Ingenia Elition X Model Numbers (REF)
(1) 782118(2) 782144
- Lot codes and dates
3 of 3 products
Products covered by this recall # Barcodes Product as published 1 Model Numbers (REF): (1) 782118, (2) 782144 2 0088483809974600884838108677UDI-DI: (1) 00884838099746, (2) 00884838108677 3 Serial Numbers: (1) 42049, 42054, 42072, 42085, 42098, 42113, 42158, 42159, 42160, 42167, 42194, 42301, 42306, 42329, 42340, 71019, 71025, 71050, 71528, 85655, 85661, 85665, 85676, (2) 42062, 42105, 42250, 42323, 42346, 42441, 71278, 71366, 71504, 71508 - Amount recalled
- 33 units
This recall covers 19 products
The agency filed one notice per product. You are reading one of them; the other 18 are below.
6 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new produce recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.